naproxen + sumatriptan: prescribing and clinical use
Focused clinical detail for use alongside current product information, local policy and patient-specific assessment.
naproxen + sumatriptan: clinical details
Prescribing considerations
- Confirm a clear migraine diagnosis and investigate atypical or new neurological symptoms before prescribing.
- Assess cardiovascular risk and gastrointestinal, renal, hepatic, bleeding and asthma-related risks.
- Review headache frequency, as repeated acute-treatment use can contribute to medication-overuse headache.
- Not recommended for people younger than 18 or older than 65 because appropriate safety and efficacy data are lacking.
Contraindications and cautions
- Ischaemic heart disease, previous myocardial infarction, coronary vasospasm, peripheral vascular disease or severe heart failure
- Previous ischaemic stroke or transient ischaemic attack
- Moderate or severe hypertension, or uncontrolled mild hypertension
- Active or recurrent peptic ulceration, gastrointestinal bleeding, or previous NSAID-associated bleeding or perforation
- Previous asthma, angioedema, urticaria, rhinitis or similar hypersensitivity caused by aspirin or another NSAID
- Severe renal impairment or moderate-to-severe hepatic impairment
- Concurrent or recent MAOI use, another triptan, or an ergotamine-type treatment
- Third trimester of pregnancy
- Hypersensitivity to either active ingredient or an excipient
Monitoring
- Check blood pressure and investigate clinically significant chest symptoms.
- Monitor renal function where renal perfusion is vulnerable.
- Watch for gastrointestinal bleeding, ulceration, fluid retention and worsening heart failure.
- Observe for serotonin syndrome when serotonergic antidepressants or lithium are clinically necessary.
Clinical pharmacology
Sumatriptan is a selective serotonin receptor agonist that produces cranial vasoconstriction and inhibits trigeminal activity. Naproxen is an NSAID that inhibits cyclooxygenase-dependent prostaglandin production.
Formulation and product differences
- Fixed-combination, film-coated oral tablet containing sumatriptan and naproxen sodium.
- The tablet has an optimised absorption profile and must not be split, crushed or chewed.
- It can be taken with or without food.
- It contains sodium as an excipient.
naproxen + sumatriptan preparations and strengths
Tablet
Route: Oral
Strengths: 85 mg + 457 mg
naproxen + sumatriptan interactions
Check all prescribed, pharmacy and herbal products before use. Important interactions include:
Other triptans or ergotamine-type treatments
Combining their blood-vessel effects can increase the risk of coronary vasospasm and is contraindicated.
Monoamine oxidase inhibitors (MAOIs)
They can substantially increase sumatriptan exposure; concurrent or recent use is contraindicated.
SSRIs, SNRIs or lithium
These may increase the risk of serotonin syndrome; SSRIs can also increase gastrointestinal bleeding risk with naproxen.
Sources
These sources were used to prepare and review this medicine page.
Prepared and reviewed by the iatroX editorial team.